FDA Inspection 875165 - Vygon GmbH & Co. KG - March 20, 2014

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Record Details

This FDA Inspection record concerns Vygon GmbH & Co. KG, with an inspection on March 20, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company: Vygon GmbH & Co. KG
Inspection Date: March 20, 2014
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1ec8dee5-6425-4350-ab35-ded1239d1555

Violation Codes9

21 CFR 803.17(a)(1)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.20(c)21 CFR 820.2221 CFR 820.30(e)21 CFR 820.30(f)21 CFR 820.5021 CFR 820.90(b)(1)

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